Canonical Allele Identifier: PA645423144
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375977
ClinVar RCV Id: RCV000435966
ClinVar Variation Id: 376445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Phe53Leu
CA16602452
NM_002755.4:c.157T>C
CA16602880
NM_002755.4:c.159T>G
CA392929197
NM_002755.4:c.159T>A